Jobs in Exeter

Surgical Medical Sales Representative

This role involves driving new business and developing existing customer relationships in the surgical oncology implant market. Responsibilities include consultative selling in operating rooms, preparing quotations, demonstrating equipment, and attending industry events. The position offers a structured development plan and a supportive, progressive company culture.

Wallace Hind Selection Wr11Db, United Kingdom £45,000 – £50,000 pa

Field Service Engineer, Medical Diagnostic Systems

Perform on-site installation, maintenance, and repair of advanced medical diagnostic equipment in NHS and private laboratory settings. Provide technical troubleshooting and customer support, ensuring minimal downtime for critical healthcare systems. Receive full product training and work within a globally recognised leader in diagnostic technology.

TRS Consulting Kirkcaldy, Fife, KY1 1JA, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

Perform on-site service and repair of advanced medical diagnostic systems in NHS and private laboratories. Provide technical troubleshooting and support to lab staff, ensuring minimal downtime. Receive full product training and work across a range of high-value diagnostic equipment.

TRS Consulting Winchester, Hampshire, United Kingdom £52,000 pa

Product Quality Engineer

This role involves analyzing product performance data and nonconforming material for the OrganOx Metra, a Class III medical device used in organ perfusion. The engineer will lead root cause investigations, support supplier quality processes, and drive improvements to manufacturing and inspection procedures. The position requires hands-on analysis of returned devices, development of test methods, and collaboration across engineering and supplier teams to ensure product quality and patient safety.

OrganOx Oxford, United Kingdom

On-site Permanent

Software Test Manager

The Software Test Manager leads the testing of software for medical devices, ensuring rigorous testing, compliance, and patient safety. Responsibilities include managing a team of test engineers, implementing CI/CD, and engaging with regulatory bodies and external stakeholders.

OrganOx Oxford, United Kingdom

On-site Permanent

Sales Specialist CT

Act as a clinical and technical expert for Philips' Computed Tomography (CT) solutions, supporting Account Managers with sales enablement, customer engagement, and solution configuration. Deliver technical presentations, contribute to tender strategies, and provide market feedback to shape product offerings. Work remotely across the UK&I region with frequent travel to customer sites in healthcare settings.

Philips Rushmoor, GU14 7JT, United Kingdom

Clinical Scientist MR

This role involves supporting research collaborations across multiple UK sites, managing customer relationships, and contributing to the development of Philips MRI products. Responsibilities include scientific leadership, project management, and knowledge transfer within a Europe-wide team of Clinical Scientists.

Philips United Kingdom

Senior Regulatory Affairs Specialist

This role involves managing regulatory compliance for advanced wound care medical devices throughout their lifecycle, including preparing global regulatory submissions, guiding product development teams, and liaising with regulatory authorities. The specialist ensures adherence to standards such as ISO 13485, FDA 21 CFR Part 820, cGMP, and cGDP, while reviewing product documentation and supporting continuous improvement. Based in Hull, the position operates within a collaborative, global team environment focused on bringing innovative healthcare products to market.

Smith & Nephew United Kingdom

Hybrid Permanent

Senior Analytical Chemist

Perform analytical testing of raw materials, intermediates, and finished medical products using techniques like ICP, GC, IR, UV-Vis, and TOC. Ensure QA compliance through method validation, equipment calibration, and stability testing, while supporting OOS/OOT investigations and continuous improvement initiatives. Work within a regulated laboratory environment to maintain quality standards and regulatory requirements.

Smith & Nephew United Kingdom

Medical Safety Officer - Solid Tumors

The Medical Safety Officer (MSO) is responsible for assessing the medical safety of Innovative Medicine products and leading cross-functional teams in safety and benefit risk management. Key responsibilities include safety surveillance, risk management, and communication with stakeholders, including Health Authorities and external key opinion leaders.

Johnson & Johnson MedTech High Wycombe, United Kingdom

Graduate Trainee Engineer

This role involves joining a two-year graduate programme at Johnson & Johnson MedTech in Leeds, focusing on the development and manufacturing of orthopaedic implants. You will work across R&D, Quality, Operations, and Manufacturing teams, gaining hands-on experience in product design, process development, and continuous improvement. The programme offers extensive training, mentorship, and opportunities for professional development.

Johnson & Johnson MedTech Leeds, United Kingdom

On-site Permanent

Mechanical Engineer - Programme Manager - Drug Delivery Devices

Mechanical Engineer - Programme Manager - Drug Delivery DevicesA period of significant growth has created an opportunity for a Programme Manager with a strong Mechanical Engineering background and deep, hands‑on experience in drug delivery device development. Based in Cambridge, you...

Newton Colmore Cambridge, United Kingdom

Permanent

Quality Engineer

This role involves hands-on quality engineering within a regulated medical device manufacturing environment, focusing on improving the Quality Management System (QMS) through data-driven insights and direct collaboration with production teams. The engineer will lead non-conformance investigations, support audits, drive continuous improvement initiatives, and ensure compliance with ISO 13485 and ISO 14971 standards. Emphasis is placed on practical, floor-based problem-solving to embed a quality-first culture across operations.

Aurora Life Sciences Leeds, West Yorkshire, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Regulatory Affairs Specialist - Medical Devices - Cambridge

This role involves providing regulatory guidance across the full product development lifecycle, supporting multidisciplinary teams in a technology-driven environment. You will interpret global regulations including ISO 13485, ISO 9001, and FDA 21 CFR 820, ensuring compliance while enabling innovation. The position is embedded in project work, offering real-time input on regulatory strategy and contributing to quality management systems across medical and non-medical sectors.

Newton Colmore Cambridge, United Kingdom

Hybrid Permanent

Senior Design Assurance Engineer

This role involves ensuring medical device designs comply with global regulatory standards throughout the product development lifecycle. You'll lead design assurance activities including risk management, design controls, and verification/validation, working closely with engineering and quality teams. The position emphasizes compliance with ISO 13485, ISO 14971, and 21 CFR Part 820 within a highly regulated environment.

SRG Cambridge, Cambridgeshire, United Kingdom £60,000 – £70,000 pa